Frank N, Bertram B, Frei E, Hadjiolov D, Wiessler M
Institute of Toxicology and Chemotherapy, German Cancer Research Center, Heidelberg.
Carcinogenesis. 1988 Jul;9(7):1303-6. doi: 10.1093/carcin/9.7.1303.
Diethyldithiocarbaminate (DDTC), mercaptoethanesulfonate (MESNA) and ethylxanthate (PEX) were tested for their influence on N-nitrosodiethylamine (NDEA) metabolism. The exhalation rate of 14CO2 released from [14C]NDEA was decreased by PEX, but not by MESNA or DDTC. The sulfur compounds led to an increased excretion of unchanged NDEA in urine in the order PEX greater than DDTC much greater than MESNA. The activity of NDEA-deethylase in liver microsomal system was decreased only after DDTC or PEX treatment. Glutathione content and glutathione-S-transferase activity were not affected significantly by any of the tested compounds. NDEA-induced single-strand breaks in liver cell DNA were inhibited after PEX treatment.
测试了二乙基二硫代氨基甲酸盐(DDTC)、巯基乙磺酸盐(MESNA)和乙基黄原酸盐(PEX)对N-亚硝基二乙胺(NDEA)代谢的影响。PEX降低了从[14C]NDEA释放的14CO2的呼出率,但MESNA或DDTC没有这种作用。这些含硫化合物导致尿液中未变化的NDEA排泄增加,顺序为PEX>DDTC>>MESNA。仅在DDTC或PEX处理后,肝微粒体系统中NDEA-脱乙基酶的活性降低。所测试的任何化合物均未显著影响谷胱甘肽含量和谷胱甘肽-S-转移酶活性。PEX处理后,NDEA诱导的肝细胞DNA单链断裂受到抑制。